Finished product reference

Potassium Citrate

Tablet · Oral · 5 mEq

List code
51901
Pharmacologic class
Urinary alkalinising agent / potassium supplement

What it is and how it works

Citrate is metabolised to bicarbonate, raising urinary pH and urinary citrate excretion. Increased urinary citrate binds calcium and inhibits calcium oxalate and calcium phosphate crystal formation, while alkalinisation increases the solubility of uric acid and cystine.

Indications

Prevention of calcium oxalate and uric acid kidney stones in hypocitraturia or renal tubular acidosis; urinary alkalinisation; relief of discomfort in mild urinary tract infection (effervescent/powder preparations).

Dosage and administration (summary)

Taken orally with or after meals with plenty of water; dose is adjusted to urinary citrate and pH, commonly 30–60 mmol (mEq) daily in divided doses for stone prevention.

Contraindications

Hyperkalaemia or conditions predisposing to it (severe renal impairment, untreated adrenal insufficiency), active urinary tract infection with urea-splitting organisms, and gastrointestinal obstruction or delayed transit (tablets).

Warnings and precautions

Monitor serum potassium and renal function, especially with potassium-sparing diuretics, ACE inhibitors or angiotensin II receptor antagonists. Gastrointestinal irritation may occur.

Storage and supply

Store below 25 °C in a dry place.

Source: reference summary prepared from the EU SmPC/EPAR, BNF and WHO Model Formulary. The approved product information in Iran governs.

Reference information for professional sourcing and registration enquiries, not medical advice or a promotion. Drug information is condensed from US FDA prescribing information (public domain, via openFDA and DailyMed) and does not replace the product’s approved labelling in Iran. Availability, origin and documentation are confirmed per enquiry.

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